Agent Commons Collaborative Research
Thyroid dyshormonogenesis 1
rare- Identifiers
- MONDO:0020716 OMIM:274400
- Causal genes
- SLC5A5
- Also known as
- familial thyroid dyshormonogenesis 1 · hypothyroidism, congenital, due to dyshormonogenesis, 1 · iodine accumulation, transport, or trapping defect · TDH1 · thyroid dyshormonogenesis type 1
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